A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2415
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report ; volume:17 ; number:1 ; day:18 ; month:1 ; year:2017 ; pages:1-5 ; date:12.2017
BMC ophthalmology ; 17, Heft 1 (18.1.2017), 1-5, 12.2017
- Schlagwort
-
Augenheilkunde
Augenkrankheit
- Urheber
-
Ouzzif, Zohra
- Beteiligte Personen und Organisationen
-
El maataoui, Aissam
Traore, Zeinab
Biaz, Asmae
El Machtani, Samira
Dami, Abdellah
Bouhsain, Sanae
Messaoudi, Nezha
Benchrifa, Fatiha
SpringerLink (Online service)
- DOI
-
10.1186/s12886-017-0402-x
- URN
-
urn:nbn:de:1111-201702146006
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:47 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Ouzzif, Zohra
- El maataoui, Aissam
- Traore, Zeinab
- Biaz, Asmae
- El Machtani, Samira
- Dami, Abdellah
- Bouhsain, Sanae
- Messaoudi, Nezha
- Benchrifa, Fatiha
- SpringerLink (Online service)
Ähnliche Objekte (12)
Wide-field imaging of sickle retinopathy
Sickle cell retinopathy. A focused review
Myocardial iron overload in sickle/thalassemia patients of Italian origin
Risk factors associated with sickle cell retinopathy: findings from the Cooperative Study of Sickle Cell Disease
Relationship between retinal vessel tortuosity and oxygenation in sickle cell retinopathy
Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease
Cardiac and pancreatic iron overload evaluation of sickle/β-Thalassemia patients utilizing T2* MRI
Novel Variants of CEP152 in a Case of Compound-Heterozygous Inheritance of Epilepsy
A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran
Posterior reversible encephalopathy syndrome in a known case of sickle-beta-thalassemia: a case presentation
Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency
P6.9 Measuring Arterial Stiffness Using Popmetre® in the African Heterozygous and Homozygous Sickle Cell Disease
Wide-field imaging of sickle retinopathy
Sickle cell retinopathy. A focused review
Myocardial iron overload in sickle/thalassemia patients of Italian origin
Risk factors associated with sickle cell retinopathy: findings from the Cooperative Study of Sickle Cell Disease
Relationship between retinal vessel tortuosity and oxygenation in sickle cell retinopathy
Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease
Cardiac and pancreatic iron overload evaluation of sickle/β-Thalassemia patients utilizing T2* MRI
Novel Variants of CEP152 in a Case of Compound-Heterozygous Inheritance of Epilepsy
A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran
Posterior reversible encephalopathy syndrome in a known case of sickle-beta-thalassemia: a case presentation
Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency
P6.9 Measuring Arterial Stiffness Using Popmetre® in the African Heterozygous and Homozygous Sickle Cell Disease
Wide-field imaging of sickle retinopathy
Sickle cell retinopathy. A focused review
Myocardial iron overload in sickle/thalassemia patients of Italian origin
Risk factors associated with sickle cell retinopathy: findings from the Cooperative Study of Sickle Cell Disease
Relationship between retinal vessel tortuosity and oxygenation in sickle cell retinopathy
Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease
Cardiac and pancreatic iron overload evaluation of sickle/β-Thalassemia patients utilizing T2* MRI
Novel Variants of CEP152 in a Case of Compound-Heterozygous Inheritance of Epilepsy
A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran
Posterior reversible encephalopathy syndrome in a known case of sickle-beta-thalassemia: a case presentation
Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency